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CK2 inhibitor CX4945 induces sequential inactivation of proteins in the signaling pathways related with cell migration and suppresses metastasis of A549 human lung cancer cells

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dc.contributor.authorKu, Min Jeong-
dc.contributor.authorPark, Jong Woo-
dc.contributor.authorRyu, Byung Jun-
dc.contributor.authorSon, Young-Jin-
dc.contributor.authorKim, Seong Hwan-
dc.contributor.authorLee, Sang Yeol-
dc.date.available2020-02-28T22:45:12Z-
dc.date.created2020-02-06-
dc.date.issued2013-10-15-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14216-
dc.description.abstractCasein kinase 2 (CK2) is known to be involved in various cellular processes such as cell cycle, apoptosis and proliferation. It has been reported that the inhibition of CK2 induced by recently developed small molecule CX4945 shows anti-cancer effects including anti-proliferation and anti-angiogenesis in several different cancers including prostate cancer. Here we report that migration and invasion of A549 human lung cancer cells are suppressed by the inhibition of CK2 induced by CX4945. We found that CX4945 sequentially attenuates the proteins in PI3K/Akt and MAPK pathways, two signaling pathways related with cell migration. This sequential control of signal pathways inhibits the expression of membrane type 1-matrix metalloproteinase and this leads to the selective attenuation of one of the gelatinases, MMP-2, which can degrade components of extracellular matrix, and metastasis of A549 human lung cancer cell. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.subjectMATRIX METALLOPROTEINASES-
dc.subjectKINASE CK2-
dc.subjectEXPRESSION-
dc.subjectAPOPTOSIS-
dc.subjectREGULATOR-
dc.subjectCX-4945-
dc.subjectKEY-
dc.titleCK2 inhibitor CX4945 induces sequential inactivation of proteins in the signaling pathways related with cell migration and suppresses metastasis of A549 human lung cancer cells-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000324304000026-
dc.identifier.doi10.1016/j.bmcl.2013.08.043-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.23, no.20, pp.5609 - 5613-
dc.identifier.scopusid2-s2.0-84884287257-
dc.citation.endPage5613-
dc.citation.startPage5609-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume23-
dc.citation.number20-
dc.contributor.affiliatedAuthorKu, Min Jeong-
dc.contributor.affiliatedAuthorPark, Jong Woo-
dc.contributor.affiliatedAuthorLee, Sang Yeol-
dc.type.docTypeArticle-
dc.subject.keywordAuthorCK2-
dc.subject.keywordAuthorCX-4945-
dc.subject.keywordAuthorMetastasis-
dc.subject.keywordAuthorMatrix metalloproteinases-
dc.subject.keywordAuthorHuman lung cancer-
dc.subject.keywordPlusMATRIX METALLOPROTEINASES-
dc.subject.keywordPlusKINASE CK2-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusREGULATOR-
dc.subject.keywordPlusCX-4945-
dc.subject.keywordPlusKEY-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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